Autoinflammation – Eine klinische und genetische Herausforderung
Research output: Contribution to journal › Research article › Contributed › peer-review
Contributors
Abstract
In the last two decades clinical rheumatological practice has been confronted with a steadily increasing number of autoinflammatory diseases, the immunological pathomechanisms of which have been elucidated and in part can be clinically well classified. Whereas targeted genetic diagnostics previously served to confirm a clinically suspected diagnosis, genetic sequencing technology has much improved and enables a new diagnostic approach via high-throughput sequencing, e.g., panel sequencing, whole exome and whole genome sequencing. Thus, the decision to make a diagnosis clinically and/or genetically, has become a daily challenge. This article contrasts the clinical, immunological and genetic aspects of autoinflammatory diseases.
Translated title of the contribution | Autoinflammation—A clinical and genetic challenge |
---|
Details
Original language | German |
---|---|
Pages (from-to) | 953–965 |
Number of pages | 13 |
Journal | Zeitschrift für Rheumatologie |
Volume | 80 |
Issue number | 10 |
Early online date | 12 Oct 2021 |
Publication status | Published - Dec 2021 |
Peer-reviewed | Yes |
External IDs
RIS | Horneff2021 |
---|---|
Scopus | 85116893519 |
ORCID | /0009-0003-6519-0482/work/143074874 |
Keywords
Keywords
- Hochdurchsatzsequenzierung, Next-Generation-Sequenzierung, Panel-Sequenzierung, Whole-Exom-Sequenzierung, Whole-Genom-Sequenzierung, High-throughput sequencing, Next-generation sequencing, Panel sequencing, Whole exome sequencing, Whole genome sequencing